Tethered coil for treatment of body lumens

ABSTRACT

Disclosed is an apparatus and a method for removable of undesired material from body lumens. The apparatus may be used for fragmenting or removing a thrombus or occlusion from a blood vessel. The apparatus includes first shape segments and second shape segments connected to form a coiled member. A longitudinally extending tether is positioned inside the first shape segments and outside the second shape segments along the length of the coil. Applying a proximal force on the tether produces a change in the shape of at least a portion of the coil from a first generally linear configuration to a second complex three dimensional shape. A method of using the apparatus to engage and remove, or fragment, the thrombus or occlusion is disclosed.

FIELD OF THE INVENTION

The present invention relates generally to medical devices for treatmentof body lumens. More specifically, the present invention relates tomedical devices for fragmentation and/or removal of blood clots, emboli,or other pathology from body lumens such as blood vessels.

BACKGROUND OF THE INVENTION

Medical devices and methods of treatment of an obstructed body lumen areknown in the art. Such known treatments of a body lumen includeincreasing blood flow through an occluded blood vessel by fragmenting orretrieving a thrombosis, blood clot, or embolism located within thelumen of the blood vessel. There has been recognized by those skilled inthe art a need for improved medical devices and improved methods fortreating obstructed body lumens including obstructed blood vessels.

SUMMARY OF THE INVENTION

Briefly and in general terms, the present invention provides a new andimproved apparatus for the treatment of a body lumen including atethered coil device adapted for treatment of the body lumen, includinga coiled member, having at least one first shape segment longitudinallyconnected with at least one second shape segment. The first shapesegment has a first cross sectional area and the second shape segmenthas a second cross sectional area that is less than the first crosssectional area. The coiled member has a proximal end and a distal end, afirst generally linear configuration, and a secondary generally threedimensional configuration. The device includes a tether having a distaltether portion and a proximal tether portion. The distal tether portionis connected with the coiled member of the device at an attachmentpoint, and slidingly disposed generally longitudinally inside the lumenof the first shape segment and outside the wall of the second shapesegment. The proximal tether portion extends proximally beyond theproximal end of the coiled member and is adapted for application of aproximal longitudinal force, which changes a shape of the coiled memberfrom the first generally linear configuration to the secondary generallythree dimensional configuration.

Furthermore, the present invention provides a method of treating athrombus within a region of a blood vessel, including positioning aportion of a thrombus engaging device at the region of the blood vesselto be treated. The thrombus engaging device is formed from a pluralityof first shape segments longitudinally connected with a plurality ofsecond shape segments and further includes a tether slidingly threadedbetween at least one first shape segment and one second shape segment.The method further includes transforming the portion of the thrombusengaging device from a generally linear configuration to a secondarygenerally three dimensional configuration by applying a proximallydirected force on the tether, thereby engaging the thrombus with thethrombus engaging device.

Other features and advantages of the invention will become more apparentfrom the following detailed description of preferred embodiments of theinvention, when taken in conjunction with the accompanying exemplarydrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features, aspects and advantages of the presentinvention are described with reference to drawings of a preferredembodiment, which are intended to illustrate, but not to limit, thepresent invention.

FIG. 1 is a side view of one embodiment of the body lumen treatingdevice of the present invention in a first configuration.

FIG. 2A is a cross sectional view through a first shape coil element ofthe body lumen treating device of FIG. 1.

FIG. 2B is a mid-longitudinal sectional view through a portion of afirst shape coil element of the body lumen treating device of FIG. 1.

FIG. 2C is an illustration of the cross sectional area of the firstshape coil element of FIG. 2A.

FIG. 3A is a cross sectional view through a second shape coil element ofthe body lumen treating device of FIG. 1.

FIG. 3B is a mid-longitudinal sectional view through a portion of asecond shape coil element of the body lumen treating device of FIG. 1.

FIG. 3C is an illustration of the cross sectional area of the secondshape coil element of FIG. 3A.

FIG. 4A is an illustration of the body lumen treating device of FIG. 1in a second three dimensional configuration.

FIG. 4B is an illustration of the body lumen treating device of FIG. 1in a second three dimensional configuration.

FIG. 4C is an illustration of the body lumen treating device of FIG. 1in a second three dimensional configuration.

FIG. 4D is an illustration of the body lumen treating device of FIG. 1in a second three dimensional configuration.

FIG. 5 is a side view of an embodiment of the body lumen treating deviceof the present invention further including a catheter.

FIG. 6 is a side view of an embodiment of the body lumen treating deviceof the present invention further including a catheter and a deliverymember.

FIG. 7 is an illustration of a method of use of the body lumen treatingdevice of FIG. 1, illustrating delivery of the device through a deliverycatheter to a region of obstruction.

FIG. 8 is an illustration of the method of use of FIG. 7, furtherillustrating delivery of the device through the obstruction.

FIG. 9 is an illustration of the method of use of FIG. 7, furtherillustrating delivery of the device through the obstruction. furtherillustrating expanding the device to a secondary three dimensionalconfiguration.

FIG. 10 is an illustration of the method of use of FIG. 7, furtherillustrating withdrawing the device through the obstruction. and intothe delivery catheter to remove the obstruction.

FIG. 11 is an illustration of the method of use of FIG. 7, furtherillustrating withdrawing the device and the delivery catheter from thebody lumen.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to the drawings, which are provided for purposes ofillustration and by way of example, one embodiment of the presentinvention is an apparatus for treatment of a body lumen, which isillustrated in FIGS. 1-5.

In at least one embodiment, the present invention relates to anapparatus for treating intravascular obstructions such as a blood clot,thrombus, or embolism. Although the exemplary embodiments are describedherein for intravascular use, those skilled in the art will recognizethat the apparatus may be useful in other than vascular body lumens.

Referring now to FIGS. 1-3B, one embodiment of the present invention isan apparatus 100 for treatment of intravascular obstructions. Theapparatus includes a coiled member 102 formed from alternatinglongitudinally connected segments 104 and 106, which are respectivelyformed primarily from first shape coil elements 110 and second shapecoil elements 120. The coiled member has a proximal end 112 and a distalend 114, the distal end being adapted for positioning proximate a regionto be treated, such as a thrombus or occlusion 410 (FIG. 7).

Referring now to FIGS. 2A-2C, in one embodiment, the invention includesfirst shape coil elements 110 having a generally cylindrical or ringshape, an inner lumen 116, an outer wall 118, and a cross sectional areaA₁ defined by the outer wall. The first shape coil elements arelongitudinally connected to form generally cylindrical first shapesegments 104, having the cross sectional area A₁ and a generally helicalconfiguration around the inner lumen 116.

Referring now to FIGS. 3A-3C, in at least one embodiment the inventionfurther includes second shape coil elements 120, which arelongitudinally connected to form second shape coil segments 106. In apreferred embodiment, the second shape coil elements may have a U-shape,or horseshoe shape configuration, an inner lumen 122, an outer wall 124,an indented portion 126, and a cross sectional area A₂ defined by theouter wall 124. In yet other embodiments, the second shape coil segmentsmay have other configuration and shapes. Referring more specifically nowto FIGS. 2C and 3C, in one embodiment, the cross sectional area A₁ ofthe first shape coil elements 110 is greater than the cross sectionalarea A₂ of the second shape coil elements 120. In yet other embodiments,the cross sectional area A₁ of the first shape coil elements is lessthan the cross sectional area A₂ of the second shape coil elements. Inat least one embodiment, the cross sectional shape of the first elementsis different than the cross sectional shape of the second elements.

In one embodiment, at least one second shape coil segment 106 isconfigured to be more flexible than at least one first shape coilsegment 104. Variations in flexibility of the segments 104, 106 may beprovided, for example, by altering the materials, thickness, or shapesof the segments. In at least one other embodiment, at least one firstshape segment is configured to be more flexible than at least one secondshape segment. Furthermore, not all first shape coil segments need havethe same flexibility and not all second shape coil segments need havethe same flexibility.

Referring back now also to FIG. 1, the apparatus 100 of the presentinvention further includes a longitudinally extending tether 130, whichextends generally longitudinal down the length of the apparatus 100. Theterm tether as used herein is not intended to be limiting and includesany number of substantially longitudinally extending members known inthe art including, for example, wires, twisted wires, cables, fibers,natural fibers, polymer fibers, cords, and strings. In at least oneembodiment, the tether is slidingly positioned or threaded between atleast one first shape segment 104 formed from first shape elements 110and at least one second shape segment 106 formed from second shapeelements 120.

The tether 130 includes a proximal portion 150 having a free end 155, adistal portion 145 connected with the coil member 102, and anintermediate portion 140. In a preferred embodiment, the intermediateportion 140 of the tether is generally disposed inside the inner lumen116 of the first shape segments 110 (FIGS. 2A and 2B) and outside thewall 124 of the second shape segments 120 (FIGS. 3A and 3B).

The tether 130 is connected with the coiled member 102 at least oneattachment point 134. The attachment point may be disposed on the coiledmember 102 or at a distal blunt tip 148 of the device 100. The tethermay be fixedly connected with the coil at the attachment point. Thetether may be connected to the attachment point, for example, by glue,welding, snap fits, or friction, or by other methods well known in theart. In yet another embodiment (not shown), a distal loop in the tethermay be connected with the coiled member to provide the attachment point.In at least one embodiment, the distal attachment point is located atthe distal end 114 of the coiled member 102. In yet another embodiment,the blunt tip may be configured as a distal mass formed from the samematerials as the tether. In at least one other embodiment the attachmentpoint may be disposed between the distal end 114 of the coiled member102 and the proximal end 112 of the coiled member 102. In one furtherembodiment, the apparatus 100 may include more than one tether and/ormore than one attachment point.

The intermediate portion 140 of the tether 130 is that portion of thetether that extends longitudinally from the proximal end 112 of thecoiled member 102 to the attachment point 134. In one embodiment, thetether may enter the lumen 116 of the coiled member at an entry point132 disposed at the proximal end of the coiled member. In anotherembodiment, the tether may enter the lumen 116 of the coiled member at aposition that is distal to the proximal end 112 of the coiled member.The tether further includes a proximal portion 150 having a free end155. The proximal portion of the tether 150 is that portion of thetether that extends proximally from the proximal end 112 of the coiledmember 102. The free end 155 and proximal portion 150 of the tether 130are preferably configured to remain outside of the body lumen duringtreatment with the apparatus 100. Furthermore, the free end 155 of thetether 130 is adapted for application of a substantially longitudinalproximally directed tensioning force F by a clinician. The free end ofthe tether may further be connected to a handle and/or reel (not shown)configured to assist the clinician in applying a controlled longitudinaltensioning force F to the tether 130. The coiled member is configured tobend, forming an angle greater than zero at least one first shapesegment and/or at least one second shape segment when the proximallydirected tensioning force F is applied. In yet one further embodiment,the coiled member is capable of returning to a generally linear orstraightened first configuration when the tensioning force F isreleased.

The intermediate portion of the tether 140 is generally slidingly lacedor threaded between the first shape segments 104 and the second shapesegments 106. In at least one embodiment, the tether slidingly extendslongitudinally from the proximal end 112 towards the distal end 114 ofthe coiled member 102, and the tether 140 is generally disposed withinthe inner lumen 116 of at least one first shape segment 104 and outsidethe outer wall 124 of at least one second shape segments 106.

In at least one preferred embodiment, a portion of the tether 130 isslidingly disposed within the recess 126 of the second shape segment.The positioning of the tether 130 within the recess 126 of the secondshape segment 120 is advantageous in providing a generally uniform outerdiameter of the apparatus 100. The tether 130 is disposed such that itis closer than the outer walls 118 of the coil member to the centrallongitudinal axis of the device 100. This configuration provides thatthe tether does not extend peripherally beyond the outer walls 118 ofthe first shape segments 104, thereby reducing friction between thetether and the delivery catheter 300 and facilitating delivery of theapparatus through the lumen of a delivery catheter (FIG. 5).

The coiled member 102 of the apparatus 100 has a first generally linearor straightened configuration 101 (FIG. 1) in a relaxed state.Furthermore, the coiled member of the apparatus has at least onesecondary generally three dimensional configuration 201, 202 (FIGS. 4Aand 4B) in a tensioned state. In at least one embodiment, applying theproximally directed substantially longitudinal force F upon the tether130 produces the transformation in shape from the relaxed ornon-tensioned first generally linear configuration to at least onetensioned secondary three dimensional configuration. Applying thetensioning force F upon the tether proximal portion 150, proximallydisplaces a portion of the tether 130 to a position that is proximal tothe proximal end 112 of the coil member. The longitudinal force Fthereby effectively shortens the intermediate portion 140 of the tether130, namely that portion that remains distal to the proximal end of thecoiled member, from a length L₁ to a length L₂, wherein L₂ is shorterthan L_(1.)

In at least one embodiment, at least one second shape segment 106 of thecoiled member 102 is configured to bend, thereby creating a flexionpoint at the second shape segment upon tensioning of the tether 130 byproximal force F and shortening of the intermediate portion 140 of thetether 130 from a length L₁ to a length L₂. The bending or flexing atsecond shape segment 106 produces an angle greater than zero degreesbetween a first shape segment 104 and at least one other first shapesegment, such as an adjacent first shape segment, thereby transitioningthe coiled member to at least one secondary three dimensionalconfiguration. In at least one other embodiment, at least one firstshape segment 104 of the coiled member 102 is configured to bend,thereby creating a flexion point at the first shape segment upontensioning of the tether 130 by proximal force F and shortening of theintermediate portion 140 of the tether 130 from a length L₁ to a lengthL₂. The bending or flexing at first shape segment 104 produces an anglegreater than zero degrees between a second shape segment 106 and atleast one other second shape segment 106 b, thereby transitioning thecoiled member to at least another secondary three dimensionalconfiguration.

In one further embodiment, releasing proximal force F from the tetherproximal portion 150 permits the coil 102 to return to the firstgenerally linear configuration 101. Release of proximal force F permitsthe intermediate portion 140 of the tether 130 to return towards lengthL1 from shortened length L2. The coil may urged to return to the firstgenerally linear configuration 101 by forming the coil with a preferredshape memory linear configuration, such that when the apparatus 100 isin a relaxed state, which is free of external forces applied to thetether, the coil tends to take the linear configuration. For example,the coil may be formed from materials known in the art to have shapememory properties, such as Nitinol. The coil may alternatively be formedfrom other materials such as biocompatible metals, alloys, and polymers.Alternatively or in addition to forming the coil with a preferred shapememory linear configuration 101, the coil may be urged into a generallylinear configuration by sliding the coiled member into the lumen of adelivery catheter 300 (FIG. 5).

Various secondary three dimensional configurations 201-204 may beproduced by altering such factors as the pattern of positioning of thetether 130 amongst the segments 104 and 106, the flexibility or rigidityof the first shape segments 104 or the second shape segments 106, thenumber of first shape elements 110 or second shape elements 120 persegment 104, 106, the attachment location 134 of the tether to the coil102, the amount and duration of the proximal longitudinal force F on thetether, and the frictional forces between the tether and the coil. A fewexamples of secondary three dimensional configurations are illustratedin FIGS. 4A-4D, however, those skilled in the art will recognize thatmultiple other three dimensional configurations are possible. One suchexample of a secondary complex three dimensional configuration is aflower petal configuration 201 (FIG. 4A). Another example of a secondarycomplex three dimensional configuration is a globular configuration 202(FIG. 4B). Yet another example of a secondary complex three dimensionalconfiguration is a helical configuration 203 (FIG. 4C). Still anotherexample of a secondary complex three dimensional configuration is abeehive configuration 204 (FIG. 4D). A multitude of secondary threedimensional configurations may be provided by variation in severalapparatus factors. One such factor is variation in the location of atleast one attachment point 134. Another such factor is the number oftethers 130. Still another factor is the location of the first shapesegments and the second shape segments. Yet another factor is the lengthof the first shape segments and the length of the second shape segments.Another exemplary factor is the flexibility of the first shape segmentsand the flexibility of the second shape segments. A further factor isthe angle of the helical turns of the first shape segments and thesecond shape segments. The secondary three dimensional configurationshapes illustrated and described herein are therefore meant to only beby way of example and not limiting as to the various numbers, locations,and angles of one or more bends that that can configured along thelength of the coil, thereby resulting in a plurality of secondary threedimensional shapes.

Referring now to FIG. 5, at least one other embodiment of the apparatus100 further includes a delivery catheter 300 having a proximal end 302,a distal end 304, and a lumen 301 therebetween. The distal end of thecatheter is configured to be delivered into a body lumen, such as ablood vessel, and advanced to the portion of the body lumen to betreated. In at least one embodiment, distal end 304 of the catheter maybe configured with an enlarged or enlargeable opening 306 for receivingobstructing matter therein when such obstructing matter is retrieved bythe coiled member 102. In one embodiment, coiled member 102 is longerthan the delivery catheter 300, such that during clinical use theproximal end 112 of the coiled member and the proximal portion of thetether 150 remains outside the catheter and the body lumen, wherein thecoiled member and the tether and may be manipulated by the clinician fortreatment of a patient.

In at least one embodiment, the apparatus 100 may be configured suchthat the catheter 300 is relatively rigid, thereby resisting deformationor bending of the catheter when the coiled member 102 is transformedfrom the first linear configuration 101 to the secondary threedimensional configurations 201. Therefore, in one embodiment, only theportion of the coil that extends distally from the distal end of thecatheter will assume the secondary three dimensional configuration whentensioning force F is applied to the proximal tether 150. In yet anotherembodiment, the apparatus 100 is configured such that a portion of thecatheter is flexible, wherein when the coiled member is transitionedfrom the first linear configuration 101 towards the secondary threedimensional configurations 201 by force F, the clinician can steer aportion of the catheter. The clinician may apply varying amounts offorce F to the proximal tether 150, thereby directing a portion of thecatheter in a desired direction within the body lumen.

Referring now to FIG. 6, in yet another embodiment of the apparatus 100,a delivery member 160 is connected to the proximal end of the coiledmember 102. In such an embodiment, the proximal end 112 of the coiledmember may be disposed within the catheter, but controlled by theclinician from outside the body lumen by manipulating the deliverymember. The proximal portion of the tether 150, remains outside thecatheter and may be manipulated by the clinician to apply tensioningforce F.

Referring now to FIGS. 7-10, one further embodiment of the presentinvention includes a method of treatment of an occlusion of a body lumenutilizing the apparatus 100. Although in the exemplary method describedherein the body lumen is a blood vessel, the method is applicable toremoval of undesired material from other lumens. The method may includetreatment of a total occlusion of a blood vessel or treatment of apartial occlusion of a blood vessel.

In one embodiment, the method of treatment includes percutaneouslyinserting the delivery catheter 300 into a blood vessel lumen, such asan artery lumen. The distal end 304 of the catheter is positioned, forexample using well known interventional radiology techniques, to alocation in the body lumen 400 adjacent to a region of thrombus orocclusion 410. The distal end 304 of the catheter may be positionedproximal to the thrombus or occlusion. In yet another embodiment, thedistal end of the catheter may be advanced into and/or beyond the regionof thrombus or occlusion. As is well known in the art, the proximal end302 (FIGS. 5 and 6) of the catheter preferably remains outside the bodylumen for manipulation by the clinician. The coiled member 102 of thetethered coil apparatus 100 in the first generally linear configuration101 (FIG. 1), in the relaxed state, may be delivered through the lumen301 of the delivery catheter, adjacent to the region of thrombus orocclusion. In the first generally linear configuration, the intermediateportion 140 of the tether 130 has a relaxed length L1 (FIGS. 1 and 5).

Referring more specifically now to FIG. 8, the distal end 114 of thecoiled member 102 may be advanced through the delivery catheter 300 andbody lumen 400 into and/or beyond the region of thrombus or occlusion410. The distal end 114 of the coiled member may be advanced distallybeyond the distal end of the delivery catheter. In one furtherembodiment, the distal end 304 of the catheter may be expanded to forman enlarged opening 306 for receiving the thrombus or occlusion after ithas been engaged by the coiled member.

Referring now to FIG. 9, the coiled member 102 may be transitioned intoa tensioned state by applying tensioning force F to the tether 150,thereby forming at least one secondary complex three dimensionalconfiguration 201-204 (FIGS. 4A-4D). The coiled member 102 may betransitioned into a tensioned state by the clinician apply proximallongitudinal force F (FIG. 1) upon the proximal portion 150 of thetether 130, thereby shortening the intermediate portion 140 of thetether to tensioned length L₂. The coil in the secondary threedimensional configuration may be used to engage or fragment the thrombusor occlusion 401.

Referring to FIG. 10, the coiled member 102 in the secondary threedimensional configuration may be used to engage the thrombus orocclusion and deliver it into the distal end 304 or enlarged opening 306of the delivery catheter 300 for removal from the body lumen 400. Themethod may include using more than one type of secondary threedimensional configuration during the procedure. The available secondarythree dimensional configurations may be predetermined, for example, byselecting from the apparatus factors discussed above. The secondarythree dimensional configurations for the apparatus may also be varied bythe clinician during the procedure by selecting the amount and/orduration of proximal longitudinal force F on the tether 150 and/or byvarying the amount of shortening from L₁ to L₂.

Referring finally to FIG. 1, after the occlusion or thrombus 410 hasbeen engaged, fragmented, and/or removed from the blood vessel 400, thecoiled member 102 is returned to the first generally linearconfiguration 101 by releasing the tensioning force F from the tether150, and/or by pulling the coiled member proximally into the lumen ofthe catheter 300 to straighten the coiled member.

The invention may be embodied in other forms without departure from thespirit and essential characteristics thereof. The embodiments describedtherefore are to be considered in all respects as illustrative and notrestrictive. Although the present invention has been described in termsof certain preferred embodiments, other embodiments that are apparent tothose of ordinary skill in the art are also within the scope of theinvention. Accordingly, the scope of the invention is intended to bedefined only by reference to the appended claims.

1. A tethered coil device adapted for treatment of a body lumen,comprising: a coiled member formed from a plurality of first shape coilsegments alternatingly longitudinally connected with a plurality ofsecond shape coil segments, the first shape coil segments being formedfrom a plurality of first shape coil elements longitudinally connectedtogether and having an inner lumen and a first cross sectional area, andthe second shape coil segments being formed from a plurality of secondshape coil elements longitudinally connected together and longitudinallyconnected with said plurality of first coil elements, said second shapecoil segments having an inner lumen and a second cross sectional areathat is less than the first cross sectional area, the coiled memberhaving a proximal end and a distal end, a first generally linearconfiguration, and a secondary complex three dimensional configuration;and a tether including a distal tether portion, a proximal tetherportion, and an intermediate tether portion therebetween; the distaltether portion being connected with the coiled member of the device atan attachment point, and the intermediate tether portion being slidinglydisposed generally longitudinally inside the inner lumen of at least oneof said plurality of first shape coil segments and outside the innerlumen of at least one of said plurality of second shape coil segments;the proximal tether portion extending proximally beyond the proximal endof the coiled member and adapted for application of a proximallongitudinal force, wherein application of the proximal longitudinalforce changes a shape of the coiled member from the first generallylinear configuration to the secondary complex three dimensionalconfiguration.
 2. The tethered coil device of claim 1, wherein thesecond cross sectional area is U-shaped.
 3. The tethered coil device ofclaim 1, wherein the attachment point is disposed at the distal end ofthe coiled member.
 4. The tethered coil device of claim 1, wherein theattachment point is disposed between the proximal end of the coiledmember and the distal end of the coiled member.
 5. The tethered coildevice of claim 1, wherein the first shape coil segments and the secondshape coil segments have different flexibilities.
 6. An intravasculardevice adapted for treatment of a vascular occlusion in a body,comprising: a coiled member having a proximal end and a distal end, afirst generally linear configuration in a relaxed state, and at leastone secondary complex three dimensional configuration in a tensionedstate, the coiled member including first shaped coil elementslongitudinally connected together and second shaped coil elementslongitudinally connected together, said first shaped coil elements beinglongitudinally connected with said second shaped coil elements, thefirst shaped coil elements having an inner lumen and the second shapedcoil elements having an inner lumen, and the second shaped coil elementshaving a different cross sectional area than the first shaped coilelements, the coiled member including alternating longitudinallyconnected first and second coil segments, said first shaped coilsegments being formed of said first shaped coil elements, and saidsecond shaped coil segments being formed from said second shaped coilelements; and at least one tether having an attachment with the coiledmember, said at least one tether including an intermediate tetherportion slidingly disposed generally longitudinally inside the innerlumen of at least one of said first shaped coil segments and outside theinner lumen of at least one of said second shaped coil segments, andsaid at least one tether including a tether free end that extendsproximally from the proximal end of the coiled member, wherein thetether free end is adapted for positioning outside of the body and forapplication of a tensioning force by a clinician.
 7. The intravasculardevice of claim 6, wherein the tensioning force is sufficient to changeat least a portion of the coiled member from the first generally linearconfiguration to the secondary complex three dimensional configuration.8. The intravascular device of claim 6, wherein the coiled member isconfigured to return to the first generally linear configuration fromthe secondary complex three dimensional configuration when thetensioning force is released.
 9. The intravascular device of claim 6,wherein the at least one tether is slidingly disposed within a recess inat least one of the second shaped coil elements.
 10. The intravasculardevice of claim 9, wherein the second shaped coil elements have asmaller cross sectional area than the first shaped coil elements.
 11. Amedical device adapted for intravascular treatment of a portion of ablood vessel, comprising: a longitudinal member including a plurality oflongitudinally connected first shape coil elements and a plurality oflongitudinally connected second shape coil elements and having a firstflexion point disposed along a length of the longitudinal member, theplurality of first shape coil elements being longitudinally connectedwith the plurality of second shape coil elements, the plurality of firstshape coil elements forming a plurality of first shape coil segments,the plurality of second shape coil elements forming a plurality ofsecond shape coil segments, said plurality of first shape coil segmentsand said plurality of second shape coil segments being alternatinglylongitudinally connected together, and the plurality of first shape coilelements and plurality of second shape coil elements having dissimilarcross sectional configurations; a tether having: a distal end portionattached with the longitudinal member, a proximal end portion disposedproximally to a proximal end of the longitudinal member and having afree end adapted to remain outside of the blood vessel for applicationof a substantially longitudinal proximally directed force on the tetherby a clinician, and an intermediate length portion therebetweenextending longitudinally inside a lumen of the first shape coil elementsand outside an inner lumen of the second shape coil elements, wherein afirst angle of greater than zero degrees is formed at the first flexionpoint when the substantially longitudinal proximally directed force isapplied to the tether free end.
 12. The medical device of claim 11,further including a second flexion point disposed along the length ofthe longitudinal member, a second angle of greater than zero degreesbeing formed at the second flexion point when the substantiallylongitudinal proximally directed force is applied to the tether freeend.
 13. The medical device of claim 11, further including a pluralityof flexion points disposed along the length of the longitudinal member,wherein the longitudinal member assumes at least one complex threedimensional configuration when the substantially longitudinal proximallydirected force is applied to the tether free end.
 14. The medical deviceof claim 11, further including a delivery catheter configured forreceiving a portion of the longitudinal member therein.
 15. The medicaldevice of claim 14, wherein a portion of the delivery cathetersurrounding the longitudinal member is configured to be deflected by thelongitudinal member when the substantially longitudinal proximallydirected force is applied to the tether free end.